AMN082 free base

Modify Date: 2025-08-25 16:18:57

AMN082 free base Structure
AMN082 free base structure
Common Name AMN082 free base
CAS Number 83027-13-8 Molecular Weight 465.45700
Density N/A Boiling Point 533.7ºC at 760 mmHg
Molecular Formula C28H28N2 Melting Point N/A
MSDS N/A Flash Point 321.5ºC

 Use of AMN082 free base


AMN082 free base, a selective, orally active, and brain penetrant mGluR7 agonist, directly activates receptor signaling via an allosteric site in the transmembrane domain. AMN082 free base potently inhibits cAMP accumulation and stimulates GTPγS binding (EC50 values, 64-290 nM) at transfected mammalian cells expressing mGluR7. AMN082 free base shows selectivity over other mGluR subtypes and selected ionotropic glutamate receptors. Antidepressant effects[1][2].

 Names

Name AMN 082 dihydrochloride,N,N'-Bis(diphenylmethyl)-1,2-ethanediaminedihydrochloride
Synonym More Synonyms

 AMN082 free base Biological Activity

Description AMN082 free base, a selective, orally active, and brain penetrant mGluR7 agonist, directly activates receptor signaling via an allosteric site in the transmembrane domain. AMN082 free base potently inhibits cAMP accumulation and stimulates GTPγS binding (EC50 values, 64-290 nM) at transfected mammalian cells expressing mGluR7. AMN082 free base shows selectivity over other mGluR subtypes and selected ionotropic glutamate receptors. Antidepressant effects[1][2].
Related Catalog
Target

mGluR7[1]

In Vitro Preincubation of the synaptosomes with AMN082 (1 μM) for 10 min before 4-aminopyridine treatment efficiently inhibits the 4-aminopyridine-evoked release of glutamate, without altering the basal release of glutamate[2].
In Vivo AMN082 (6 mg/kg; p.o.) induces stress hormone increases in an mGluR7-dependent fashion in mGluR7+/+ mice (C57BL/6 genetic background)[1]. AMN082 (1.25-5.0 mg/kg, i.p.; 30 min before every Cocaine or Morphine injection during repeated drug administration or before Cocaine or Morphine challenge) dose-dependently attenuates the development, as well as the expression of Cocaine or Morphine locomotor sensitization[3].
References

[1]. Mitsukawa K, et al. A selective metabotropic glutamate receptor 7 agonist: activation of receptor signaling via an allosteric site modulates stress parameters in vivo. Proc Natl Acad Sci U S A. 2005;102(51):18712-18717.

[2]. Wang CC, et al. Metabotropic glutamate 7 receptor agonist AMN082 inhibits glutamate release in rat cerebral cortex nerve terminal. Eur J Pharmacol. 2018;823:11-18.

[3]. Jenda M, et al. AMN082, a metabotropic glutamate receptor 7 allosteric agonist, attenuates locomotor sensitization and cross-sensitization induced by cocaine and morphine in mice. Prog Neuropsychopharmacol Biol Psychiatry. 2015;57:166-175.

 Chemical & Physical Properties

Boiling Point 533.7ºC at 760 mmHg
Molecular Formula C28H28N2
Molecular Weight 465.45700
Flash Point 321.5ºC
Exact Mass 464.17900
PSA 24.06000
LogP 8.13060

 Safety Information

HS Code 2921590090

 Precursor & DownStream

Precursor  1

DownStream  0

 Customs

HS Code 2921590090
Summary 2921590090. other aromatic polyamines and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Synonyms

N,N'-diazenediyl-bis-phthalimide
1,4-bis-phthaloyltetrazene
N,N'-Dibenzhydryl-aethylendiamin
N,N'-dibenzhydryl-ethane-1,2-diamine
1,4-Bisphthalyl-tetrazen
N,N'-dibenzhydryl-ethylenediamine
Phthalimide,N,N'-azodi
AMN 082
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